A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260426



Internal ID20827466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160502457..160502914hg38UCSC Ensembl
chr3:160220245..160220702hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561169
Supporting Variants
Samples
Known GenesKPNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260426
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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